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Gene targeting of the adaptor molecule DAP12 in mice caused abnormal distribution and impaired antigen presentation capacity of dendritic cells (DCs). However, the DAP12-associated receptors expressed on DCs and their functions have not been identified yet. Here we show that the triggering receptor expressed on myeloid cells-2 (TREM-2) is a cell surface receptor on human monocyte-derived DCs, which is associated with DAP12. TREM-2/DAP12 promotes upregulation of CC chemokine receptor 7, partial DC maturation, and DC survival through activation of protein tyrosine kinases and extracellular signal–regulated kinase. In contrast to Toll-like receptor-mediated signaling, TREM2/DAP12 stimulation is independent of nuclear factor-κB and p38 stress-activated protein kinase. This novel DC activation pathway may regulate DC homeostasis and amplify DC responses to pathogens, explaining the phenotype observed in DAP12-deficient mice.
Dendritic cells (DCs) are a distinct population of bone marrow–derived leukocytes that initiate primary and secondary immune responses 1. DCs migrate from the blood to peripheral tissues, where they reside in an immature state, awaiting antigen encounter. Upon antigen capture, DCs process them into peptides, which are loaded onto MHC molecules for presentation to T cells. As a result of pathogen invasion, inflammation, and tissue damage, DCs receive additional activating signals, which induce a profound change in DC phenotype and functions, known as maturation 123. Mature DCs express the chemokine receptor CCR7, which interacts with the chemokines CCL19 (also known as EBI-1 ligand chemokine [ELC], or macrophage inflammatory protein 3 β [MIP-3β]) and CCL21 (also known as secondary lymphoid tissue chemokine [SLC], or 6-C-Kine) 456789. These chemokines are crucial for guiding DCs from peripheral tissues to draining lymph nodes, as demonstrated in mice with natural or targeted genetic deletions of CCL19, CCL21, or CCR7 1011121314. In addition, mature DCs express high levels of stable MHC-peptide complexes on the cell surface, upregulate costimulatory and adhesion molecules, and downregulate antigen-capturing molecules. Thus, mature DCs can efficiently present antigens and stimulate virgin-T cells located in the T cell–rich areas of lymph nodes 115. Here, DCs receive further activating signals from cognate Th cells, which express CD40 ligand (CD40L) 16, OX40 1718, and TNF-related activation-induced cytokine (TRANCE) 19202122. These stimuli trigger IL-12 secretion by antigen presenting DCs thus promoting Th1 type T cell responses 202324252627.
Activating signals induce DC maturation through several distinct signaling pathways. LPS, other bacterial and viral components, as well as products released by damaged tissues, activate DCs through Toll-like receptors (TLRs) 2829. TLRs trigger downstream signaling pathways, which activate the nuclear factor (NF)-κB. NF-κB promotes the transcription of a variety of genes mediating maturation 30313233. In addition, TLRs activate mitogen-activated protein kinases (MAPKs), such as the stress-activated protein kinase p38 (P38/SAPK) and the extracellular signal–regulated kinase (ERK), which concur to DC activation 2829. Inflammatory cytokines, such as IL-1, IL-18, and TNF-α, and T cell surface molecules, such as CD40L, OX40, and TRANCE, bind specific receptors that activate NF-κB as well 12034353637. A second pathway of DC maturation is initiated by the receptors for the Fc portion of IgG (FcRs), which bind antibody-opsonized pathogens 38. FcRs lack intracellular signaling motifs, but display a charged residue in the transmembrane domain, which mediates association with the γ chain of FcR (FcRγ) 39. FcRγ contains a cytoplasmic immunoreceptor tyrosine-based activation motif (ITAM), which recruits protein tyrosine kinases (PTKs) of the src and syk families. PTKs trigger protein tyrosine phosphorylation, Ca2+ mobilization, and phosphorylation of several MAPKs 4041. While FcRγ is essential for FcR-mediated DC maturation 42, the role of downstream PTKs and MAPKs is yet unknown.
Recent observations suggest that DC activation is controlled by yet another signaling pathway, which involves the adaptor molecule DAP12 (also called KARAP). DAP12 is associated with several NK and myeloid cells activating receptors 434445464748495051525354. Like FcRγ, DAP12 contains a cytoplasmic ITAM, recruits the PTKs ZAP70 and p72/syk, and promotes activation of ERK 44455556. Knock-in mice bearing a nonfunctional mutation within the ITAM of DAP12 showed a dramatic accumulation of DCs in mucocutaneous epithelia and were resistant to hapten-specific contact sensitivity 57. In addition, DAP12-deficient mice were resistant to experimental autoimmune encephalomyelitis (EAE) induced by immunization with myelin oligodendrocyte glycoprotein peptide 58. These phenotypes suggested a role of DAP12 in regulating migration and antigen presentation capacity of DCs. Three DAP12-associated receptors have been identified in myeloid cells. One of these, myeloid DAP12-associating lectin-1 (MDL-1), is a member of the C-type lectin superfamily 50. The others, signal-regulatory protein β (SIRP-β) and triggering receptor expressed on myeloid cells-1 (TREM-1), belong to the Ig superfamily 5359. TREM-1 is preferentially expressed on neutrophils and a subset of blood monocytes 53. SIRP-β and MDL-1 are mainly expressed on blood monocytes and macrophages 5060. When monocytes are differentiated toward DCs by culturing them in vitro in the presence of GM-CSF and IL-4, expression of MDL-1, SIRP-β, and TREM-1 is completely downregulated 505360.
Recently, we have cloned a cell surface receptor distantly related to TREM-1 called TREM-2. TREM-2 is a member of the Ig-superfamily characterized by a single V-type extracellular domain, a transmembrane region with a charged residue of lysine and a short cytoplasmic tail with no signaling motifs 53. Here we found that TREM-2 is associated with DAP12 and, in contrast to TREM-1, SIRP-β, and MDL-1, is not expressed on monocytes, but it is strongly upregulated on human DCs derived in vitro from monocytes. This observation provided the opportunity to investigate the role of TREM2/DAP12-mediated signaling pathways in DC migration and maturation.
Soluble TREM-2 was produced as a chimeric protein consisting of TREM-2 extracellular domain and human IgM constant regions (TREM-2 human IgM [TREM-2-HuIgM]), as previously described 61. TREM-2 extracellular domain was amplified from the cloned full length cDNA by polymerase chain reaction using the following oligonucleotides: 5′-ACTCTGCTTCTGCCCTTGGCTGGGG, 3′-tagtagGTCGACATACTTACCGGGTGGGAAAGGGATTTCTCCTTCCAA. Purification of TREM-2-HuIgM from culture supernatants was performed by affinity chromatography on Sepharose-coupled mouse anti–human IgM mAb (Sigma-Aldrich) according to manufacturer's protocols.
293 cells were transiently transfected with a cDNA encoding human TREM-2 as a FLAG peptide NH2-terminal fusion protein (Eastman Kodak Co.) using cytofectene (Bio-Rad Laboratories).
6-wk-old BALB/c mice (Iffa-Credo) were immunized with purified TREM-2-HuIgM. Spleen cells were fused with the SP2/0 myeloma cells and hybridoma supernatants were screened by ELISA using TREM-2-HuIgM as capturing protein and human-adsorbed horseradish peroxidase (HRP)-labeled goat anti–mouse IgG (BD PharMingen) as detecting Ab. ELISA-positive hybridoma supernatants were then tested by flow cytometry for staining 293 cells expressing FLAG-tagged TREM-2. mAb 29E3 (anti–TREM-2, IgG1,κ), mAb 21C7 (control IgG1, κ, anti–TREM-1) 53, and mAb 1B7.11 (control IgG1, κ, anti-2,4,6 TNP; American Type Culture Collection) were purified using GammaBind-Sepharose (Amersham Pharmacia Biotech). Purified mAbs were either biotinylated (Roche) or labeled with Cy5 (Amersham Pharmacia Biotech) according to manufacturer's protocols. F(ab′) or F(ab′)2 fragments of mAb 29E3 and mAb 21C7 were prepared using the F(ab′)/F(ab′)2 Kit (Pierce Chemical Co.). F(ab′) and F(ab′)2 were separated from the Fc portion by affinity chromatography on protein G-sepharose, followed by gel filtration on a Superdex 75 HR10/30 (Amersham Pharmacia Biotech). F(ab′) and F(ab′)2 preparations were tested for the absence of Fc fragments by immunoassay. F(ab′) and F(ab′)2 fragments were biotinylated allowing for crosslinking by ExtrAvidine (Sigma-Aldrich) or flow cytometry by Streptavidin-allophycocyanin (APC) or -PE (BD PharMingen). Alternatively, F(ab′)2 fragments were crosslinked using a goat anti–mouse IgG F(ab′)2 specific antibody (The Jackson Laboratory).
PBMCs were purified from human blood by gradient density centrifugation on lymphocyte separation medium (LSM; ICN Biomedicals/Cappel). CD14+ monocytes were purified from PBMCs by magnetic cell sorting (MACS) using CD14 MicroBeads (Miltenyi Biotec). Monocyte-derived DCs were prepared from purified monocytes as described previously 6263.
Before staining, all cells were preincubated with PBS-20% human serum for 1 h on ice to block Fc receptors (FcR). Monocytes cultured in M-CSF or GM-CSF and IL-4 were stained with either mAb 29E3, mAb 21C7, or mAb 1B7.11, followed by human-adsorbed PE-conjugated goat anti–mouse IgG (Southern Biotechnology Associates, Inc.). In three-color stainings, immature DCs cultured with LPS (100 ng/ml), TNF-α (10 ng/ml), or CD40L-transfected J558L cells 64 were incubated with Cy5-labeled mAbs 29E3 and FITC-conjugated anti-CD83 mAb (Immunotech). Cells were analyzed on a FACSCalibur™ cytometer using CELLQuest™ software (Becton Dickinson). Dead cells were excluded by gating on PI-negative cells.
Human IgG, F(ab′)2 29E3 (anti–TREM-2 mAb), or control F(ab′)2 (21C7 anti–TREM-1 mAb) were coated for 6 h at 37°C on 96-well flat-bottom plates with a final concentration of 20 μg/ml in PBS. LPS was used at a final concentration of 1 μg/ml. Immature DCs were plated at a concentration of 5 × 105 cells/well and simultaneous contact to the plate was induced by short centrifugation (400 g, 1 min, 25°C). Supernatants and cells were collected after 6, 12, 24, 36, 48, or 72 h and tested by ELISA or flow cytometry. In blocking experiments, inhibitors (PD98059 [20 μM], LY294002 [10 μM], SB203580 [2 μM], PP2 [1 μM]; all from Calbiochem), and TPCK (20 μM; Sigma-Aldrich) were added 60 min before stimulation.
To measure stimulation-dependent changes in the expression of cell surface markers and cytokine secretion, monocyte-derived DCs were stimulated as described above for 6, 12, 24, 48, and 72 h. Supernatants were collected and tested for production of IL-6, IL-8, IL-10, TGF-β, IL-12p40, IL-12p75, IL-13, IL-15, IL-18, IL-1α, IL-1β, TNF-α, and MCP-1 by ELISA (BD PharMingen). Cells were harvested and stained with anti–TREM-2, -MHC class I, -MHC class II, -CD1a, -CD11a, -CD11b, -CD11c, -CD29, -CD32, -CD35, CD38-, CD40-, -CD41, -CD54, -CD61, -CD64, -CD80, -CD83, -CD86, -CD89, -CD103, -CD115, -CD116, -CCR5, -CCR6, -CXCR4, or -Mannose receptor conjugated with Cy5-, PE-, or FITC (all from Immunotech and BD PharMingen). Anti-CCR7 mAb (BD PharMingen) was followed by F(ab′)2 PE-labeled goat anti–mouse IgM Ab (Southern Biotechnology Associates, Inc.). Stained cells were analyzed by flow cytometry.
Monocyte-derived DCs were loaded with Indo-1 AM (Sigma-Aldrich) for 30 min at 37°C, washed three times, and resuspended in RPMI/10 mM HEPES/5% FCS. Cytoplasmic Ca2+ levels were monitored in individual cells by measuring 405/525 spectral emission ratio of loaded Indo-1 dye by flow cytometry. After a baseline was acquired for at least 30 s, 29E3, 21C7, F(ab′) 29E3, F(ab′) 21C7, F(ab′)2 29E3, or F(ab′)2 21C7 were added to a final concentration of 1 μg/ml and analysis was continued up to 512 s. All antibodies and antibody fragments were biotinylated. In some experiments, ExtraAvidine (Sigma-Aldrich) was added as crosslinker together with the biotinylated primary antibodies or Ab fragments.
Monocyte-derived DCs (106 cells per time point) were stimulated as described above. After 0 (unstimulated control), 1, 2, 5, 10, and 20 min cells were harvested and chilled on ice. Cells were spun down and lysed in reducing sample buffer. Specific induction of tyrosine phosphorylation and phosphorylation of ERK, p38/SAPK, and JNK was determined by reducing Western blot analysis using anti–phospho-ERK, anti-ERK, anti–phospho-p38/SAPK, anti-p38/SAPK, anti-phospho-JNK, and anti-JNK antibodies (all from New England Biolabs, Inc.).
Monocyte-derived DCs were washed three times in PBS followed by incubation with sulfo-NHS-biotin according to the manufacturer's protocol (Pierce Chemical Co.). For pervanadate treatment, cells were incubated with 200 μM pervanadate and 200 μM H2O2 at 37°C for 5 min. Biotinylation or pervanadate stimulation was stopped by washing the cells three times in PBS/10% FCS/200 μM pervanadate and one time with ice cold PBS/200 μM pervanadate, respectively.
Surface-biotinylated cells were lysed in 1% digitonin, 100 mM Tris-HCl, pH 7.4, 150 mM NaCl, protease inhibitors (Complete; Roche Molecular Biochemicals). After overnight preclearing with normal mouse serum coupled to protein G Sepharose 4B (Amersham Pharmacia Biotech), lysates were subjected to immunoprecipitation with 5 μg/ml of 29E3, 21C7, or 1B7.11 at 4°C for 3 h. Immunocomplexes were precipitated by addition of protein-G-Sepharose 4B for 3 h at 4°C. Precipitates were washed four times with lysis buffer, followed by a final wash with 0.5% digitonin, 100 mM Tris-HCl, pH7.4, 150 mM NaCl. After separation by SDS-PAGE, precipitates were analyzed by Western blot with HRP-conjugated streptavidin. In deglycosylation experiments the precipitates were incubated for 18 h with or without N-Glycanase F (Roche) according to the manufacturer's protocol. Pervanadate-treated cells were subjected to immunoprecipitation as described above. Immunoprecipitates were analyzed by Western blot with antiphosphotyrosine PY20-HRP (Transduction Laboratories) or anti-DAP12 rabbit antiserum followed by human/mouse-adsorbed anti–rabbit IgG-HRP (Southern Biotechnology Associates, Inc.).
Monocyte-derived human DCs (107) were treated for 24 h with F(ab′)2 21C7, F(ab′)2 29E3 coated on plastic (20 μg/ml), or LPS (1 μg/ml). Cells (5 × 105 in 100 μl IMDM/0.5% BSA) were incubated for 1 h at 37°C. Cells were subsequently loaded into collagen-coated Transwells (Costar; 3-μm pore filter), which were placed onto 24-well plates containing 450 μl medium supplement with 100 ng/ml CCL19 (ELC/MIP-3β) or CCL20 (6-C-Kine/SLC) (both from PeproTech). After an incubation period of 4 h at 37°C, cells that had migrated to the lower chamber were collected and counted on a cytofluorimeter (FACSCalibur™, constant time acquisition; Becton Dickinson). In blocking experiments cells were preincubated with anti-CCR7 mAb (10 μg/ml) and added to the Transwell.
Determination of DNA fragmentation was performed as described previously 65. Inhibitors of kinases or serine proteases (PD98059 [20 μM], LY294002 [10 μM], TPCK [20 μM]) were added 60 min before stimulation. Inhibitors had no effect on cell viability or the rate of constitutive apoptosis at the indicated concentrations.
Nuclear extracts were prepared according to the method of Schreiber et al. 66 with some modifications. Stimulation of monocyte-derived human DCs (107) with control or anti–TREM-2 antibody or with LPS was performed for 0.5 or 4 h at 37°C as described above. Cells were washed in PBS, resuspended in 10 ml of ice-cold buffer A (10 mM Tris-HCl, pH 7.9, 60 mM KCl, 1 mM EDTA, 0.75 mM spermidine, 0.15 mM spermine, 1 mM DTT, 0.5 mM PMSF, 1 μg/ml aprotinin, 1 μg/ml leupeptin, and 1 μg/ml pepstatin), and incubated for 15 min on ice. Nonidet P-40 was added from a 10% stock solution to a final concentration of 0.6%, and samples were vortexed for 10 s. After incubation for 3 min on ice, samples were centrifuged at 3,000 rpm for 10 min at 4°C. Nuclei were washed in 10 ml of ice-cold buffer A and resuspended in 30 ml of ice-cold buffer C (20 mM Tris-HCl, pH 8, 0.4 M NaCl, 1.5 mM MgCl2, 1 mM EDTA, 1 mM DTT, 0.5 mM PMSF, 1 μg/ml aprotinin, 1 μg/ml leupeptin, 1 μg/ml pepstatin, and 25% glycerol). Nuclei were incubated for 30 min at 4°C, and nuclear extracts were separated from debris by centrifugation at 15,000 g for 15 min at 4°C. Protein concentrations were determined by Bradford assay using Bio-Rad protein assay (Bio-Rad Laboratories). NF-κB consensus and mutant binding sites were 5′-AGTTGAGGGGACTTTCCCAGGC-3′ and 5′-AGTTGAGGCGACTTTCCCAGGC-3′, respectively. Annealed binding sites were radiolabeled using polynucleotide T4 kinase and γ[32P]-ATP. Radiolabeled oligonucleotides were purified by electrophoresis through an 8% polyacrylamide gel containing 22.5 mM Tris-borate and 0.5 mM EDTA, overnight elution from gel slices at 37°C, concentration using Elutip-d columns (Schleicher & Schuell), and ethanol precipitation. Electrophoretic mobility assays (EMSAs) were performed as described previously 67 with some modifications. Nuclear extracts (2 μg) were incubated with 1 μg of poly(dI-dC) carrier and 1 μg of BSA in a 25 μl reaction mix containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, 1 mM DTT, 1 mM EDTA, and 5% glycerol for 10 min at 4°C in the presence or absence of 25-fold excess of unlabeled oligonucleotide competitors. Labeled binding-site probes (15 fmols, ~5 × 104 cpm) were then added for an additional 20 min of incubation at 4°C. Samples were electrophoresed through a 4% polyacrylamide gel containing 22.5 mM Tris-borate and 0.5 mM EDTA at 4°C.
In initial studies, TREM-2 transcript was selectively detected in monocyte-derived DCs by reverse transcriptase (RT)-PCR (data not shown). To precisely investigate the cellular distribution of TREM-2 as well as its biochemical characteristics and functions, we produced an anti–TREM-2 mAb (29E3). This antibody stained TREM-2–transfected 293 cells specifically, compared with control transfectants (Fig. 1 A). In agreement with RT-PCR data, TREM-2 was highly expressed on DCs derived from peripheral blood monocytes upon in vitro culture with GM-CSF and IL-4 (Fig. 1 B). DC maturation induced by LPS, TNFα, CD40L-expressing cells (Fig. 1 C), IL-1β, CpG oligonucleotides, or aggregated IgG (data not shown) led to complete downregulation of TREM-2. TREM-2 was undetectable on macrophages obtained by culturing monocytes up to 14 d with M-CSF (Fig. 1 B) and on primary DCs of peripheral blood (data not shown). Thus, TREM-2 is preferentially expressed on immature monocyte-derived DCs.
Immunoprecipitation of TREM-2 from surface-biotinylated monocyte-derived DCs revealed that TREM-2 is a glycoprotein of ~40 kD, that is reduced to 26 kD after N-deglycosylation (Fig. 2 A). This result is in agreement with the predicted molecular mass of TREM-2 53. As TREM-2 lacks known signaling motifs in the cytoplasmic domain and displays a charged residue of lysine in the transmembrane domain 53, it was likely to be associated with a separate adaptor molecule to transduce signals. Adaptor molecules, such as DAP12, DAP10, and FcRγ are tyrosine phosphorylated upon cell treatment with the phosphatase inhibitor pervanadate 446869. Indeed, anti-phosphotyrosine blotting of TREM-2 immunoprecipitates from pervanadate-stimulated monocyte-derived DCs revealed a phosphorylated protein of ~14 and ~28 kD under reducing and nonreducing conditions, respectively (Fig. 2 B). This pattern was consistent with the association of TREM-2 with a tyrosine-phosphorylated protein that forms a disulfide-linked homodimer. Immunoblotting of TREM-2 immunoprecipitates with anti-DAP12, -DAP10, and -FcRγ antisera demonstrated that TREM-2, like TREM-1, associates only with DAP12 (Fig. 2 C, and data not shown). Thus, TREM-2 is capable of stimulating DAP12-linked signaling pathways in DCs.
To see whether the TREM-2/DAP12 complex transduces activating signals in DCs as other DAP12-associated receptors do in NK cells and neutrophils 43444547484950515253545670, we stimulated TREM-2 with 29E3 mAb or with its F(ab′)2 fragment. In both cases, ligation of TREM-2 elicited a rapid rise in intracellular Ca2+ concentration of DCs (Fig. 3 B). However, monovalent engagement of TREM-2 using F(ab′) 29E3 did not induce calcium mobilization, indicating that TREM-2–mediated activation needs at least two or more receptors crosslinked (data not shown). Cross-linking of TREM-2 with F(ab′)2 29E3 stimulated tyrosine phosphorylation of several proteins with approximate molecular masses of ~110, ~90, ~60–70, and ~30–40 kD (Fig. 3 C). The observed ~40 kD tyrosine phosphorylated proteins corresponded to the ERK1/2, as demonstrated by antiphospho-ERK1/2 immunoblotting (Fig. 3 D). It was previously shown that survival of LPS-stimulated DCs is dependent on ERK 71 and phosphatidylinositol 3-kinase (PI-3K) 72, while maturation is mainly mediated through NF-κB. Therefore, we tested whether stimulation of TREM-2 leads to prolonged survival of DCs kept in culture in the absence of GM-CSF or IL-4. As shown in Fig. 3 E, crosslinking of TREM-2 with F(ab′)2 29E3 prolonged DC survival for almost 8 d. Treatment of TREM-2–stimulated DCs with the ERK inhibitor PD98059 blocked this survival effect. Inhibitors of PI-3K, IκB-phosphorylation, or IκB-degradation had no effect (Fig. 3 F, and data not shown). These observations indicate that TREM-2 induces survival of DCs through activation of the ERK pathway.
To examine whether TREM-2 can trigger migration of DCs and/or their maturation into efficient antigen-presenting cells, immature DCs were stimulated with F(ab′)2 29E3 mAb coated on plastic surface. These cells were tested for the expression of cell surface molecules involved in migration, antigen presentation, costimulation, and adhesion, as well as for the production of cytokines. Upon TREM-2 ligation, CCR7 surface expression was rapidly increased (Fig. 4 A). CCR7 was functionally competent, as TREM-2–stimulated DCs showed a specific chemotactic response towards the CCL19 and CCL21, which could be inhibited by anti-CCR7 mAb (Fig. 4 B). The amplitude and kinetics of CCR7 upregulation induced via TREM-2 were different compared with those induced by LPS stimulation (Fig. 4 A). While expression of CCR7 was detectable by 6 h after TREM-2 stimulation, LPS-induced upregulation of CCR7 was weaker and occurred only after 24 h of cell stimulation. Regardless of CCR7 surface levels, however, LPS-stimulated DCs displayed a stronger chemotactic response toward CCL19 and CCL21 than TREM-2–stimulated DCs. Therefore, DC mobility and chemotaxis to CCL19 and CCL21 is not solely related to CCR7 expression levels. Indeed, it has been shown that other receptors, such as the multidrug resistance-associated protein 1, can contribute to optimal mobilization of DCs from skin to secondary lymphoid organs 73.
Ligation of TREM-2 also induced increased cell surface expression of several molecules involved in T cell stimulation, such as MHC class II, CD40, and CD86 (Table ). In contrast to LPS-activated DCs, CD83 and intracellular adhesion molecule (ICAM)-1 were not upregulated. Furthermore, antigen-capturing molecules, such as CD32, CD64, CD89, and the mannose receptor, were not downregulated (Table ). DCs activated through TREM-2 did not secrete either IL-12, or other cytokines (Table ). Thus, TREM-2 mediates a unique pattern of DC activation, characterized by upregulation of CCR7, expression of some T cell stimulatory molecules, and lack of cytokine secretion.
LPS-induced maturation of DCs requires the activity of NF-κB transcription factor 747576. Prior to activation, NF-κB is retained in the cytoplasm through binding to the inhibitory IκB protein. Stimulation of cells with LPS leads to IκB kinase (IKK)-mediated phosphorylation of IκB. This is followed by rapid ubiquitination and proteolytic degradation of IκB, allowing nuclear translocation of NF-κB and binding to κB-promoter elements 3031323377. To study whether TREM-2 activates the IκBα/NF-κB pathway, we stimulated DCs through TREM-2 and analyzed the phosphorylation of IκBα by Western blot analysis. In addition, we assessed the nuclear translocation of NF-κB by searching for NF-κB–containing complexes in EMSAs. In striking contrast to LPS 72, antibody-mediated ligation of TREM-2 did not lead to phosphorylation and degradation of IκBα (Fig. 5 A) or nuclear translocation of NF-κB (Fig. 5 B). It was previously shown that LPS-induced maturation of DCs is also mediated by activation of p38/SAPK 7278. To see whether TREM-2 activates p38/SAPK, we crosslinked TREM-2 on DCs with F(ab′)2 29E3 and analyzed tyrosine phosphorylation of p38/SAPK by Western blot analysis. In contrast to LPS, TREM-2 did not induce p38/SAPK tyrosine phosphorylation (Fig. 5 C). Thus, the TREM-2–induced activation pathway is NF-κB- and p38/SAPK independent.
To further characterize the signaling molecules involved in TREM-2–mediated DCs maturation, DCs were incubated with inhibitors of ERK (PD98049), NF-κB (TPCK), p38/SAPK (SB203580), and PTKs (PP2). Treated cells were stimulated with either F(ab′)2 anti–TREM-2 mAb, LPS, or immobilized IgG and subsequently analyzed for cell surface expression of maturation markers, such as CCR7, MHC class II, ICAM-1 CD83, CD40, and CD86. TREM-2 induced upregulation of CCR7, CD86, class II, and CD40, while cell surface expression of ICAM-1 and CD83 was not increased (Fig. 6, red bars). Remarkably, TREM-2–induced expression of CCR7, CD86, class II, and CD40 was completely blocked by a PTK inhibitor and partially blocked by an ERK inhibitor. This differential inhibitory capacity suggests that PTK may activate downstream signaling molecules other than ERK, which concur to TREM-2–mediated DC maturation. Incubation of DCs with NF-κB and p38/SAPK inhibitors had virtually no effect (Fig. 6, red bars).
LPS-induced maturation pathway was totally distinct from that mediated by TREM-2. LPS-induced upregulation of CCR7, MHC class II, ICAM-1 CD83, CD40, and CD86 (Fig. 6, green bars) 1. Incubation of DCs with NF-κB and p38/SAPK inhibitors prevented LPS-induced maturation, whereas ERK inhibitor had a modest effect, as described previously (Fig. 6, green bars) 7278. Finally, engagement of FcR by immobilized IgG induced a maturation pattern, which was similar to that induced by TREM-2, with the exception of an upregulation of ICAM-1 (Fig. 6, blue bars). Incubation of DCs with PTK and ERK inhibitors resulted in total and partial inhibition of FcR-induced maturation, respectively. These observations provide evidence that TREM-2 mediates DC maturation by PTK/ERK-dependent pathways. These pathways overlap with those initiated by FcRs, but are distinct from the IκBα/NF-κB and p38/SAPK-dependent pathways triggered by LPS.
We have shown that TREM-2 is an activating receptor expressed on monocyte-derived DCs, which activates PTK and ERK signaling through the association with DAP12, an ITAM-containing adaptor molecule 4445. TREM-2/DAP12-mediated signaling promotes survival of DCs and upregulation of CCR7, MHC class II, CD86, and CD40. Compared with the classical DC activation triggered by LPS, the TREM2/DAP12 pathway does not lead to upregulation of ICAM-1 and CD83 or secretion of IL-12, and is entirely independent of NF-κB and p38/SAPK signaling. TREM2/DAP12-induced DC maturation is more similar to that initiated by the FcRs, through the association FcRγ, another ITAM-containing adaptor molecule 42. Indeed, here we have shown that FcR-mediated maturation is dependent on PTK and ERK signaling.
This study is the first to show that a DAP12-mediated pathway can activate human DCs. What could be the physiological significance of this maturation pathway? TREM-2 or other DAP12-associated receptors could synergize with cell surface receptors, which activate DCs through NF-κB. This possibility is consistent with previous work on TREM-1, another DAP12-associated myeloid receptor 53, which is upregulated on neutrophils upon exposure to LPS and synergizes with LPS in promoting inflammatory responses to bacterial infections 7980. Thus, DAP12-associated DC receptors could amplify maturation signals transduced by other receptors, allowing for optimal antigen presentation. DAP12-mediated DCs activation could also be important in the normal homeostasis of DCs. TREM-2 induces upregulation of CCR7, which plays a pivotal role in directing DCs from the periphery to the T cell rich areas of draining lymph nodes 1011121314. Thus, in the absence of pathogens, DAP12-associated receptors could regulate the homeostatic circulation of DCs from the periphery to the lymph nodes, allowing for renewal of lymph node DCs. In addition, TREM-2 induces upregulation of some T cell stimulatory molecules, such as MHC class II, CD40, and CD86. Thus, DAP12-mediated maturation of DCs may promote partial activation of T cells in the absence of exogenous antigens. This activation presumably is critical for the survival of T cells and the homeostasis of T cell populations 81.
We have demonstrated that crosslinking of TREM-2 promotes DC survival. This observation is consistent with previous demonstration that ERK signaling prevents apoptosis of LPS-stimulated DCs 71. In addition, we have evidence that TREM-1/DAP12 complex promotes survival of neutrophils and monocytes (unpublished data). Together, these observations suggest that DAP12-mediated pathways are critical for myeloid cell survival. Based on our data and previous studies in other systems, DAP12-mediated ERK activation is likely to induce phosphorylation of Bad or other Bcl-2 inhibitors 828384. Once released from inhibition, Bcl-2 could translocate into the mitochondria and inhibit DC apoptosis 85868788.
The physiological functions of DAP12-mediated DC activation are consistent with the reported phenotypes of knock-in mice bearing a nonfunctional DAP12 and DAP12-deficient mice 5758. ITAM-deficient DAP12-knock-in mice showed an accumulation of DCs in mucocutaneous epithelia, associated with an impaired hapten-specific contact sensitivity 57. Our data suggest that this phenotype may be explained in part by a reduced ability of DCs to upregulate CCR7 expression and to respond to CCL19 and CCL21, affecting the migration of DCs to the T cell zone of draining lymph nodes. DAP12-deficient mice were resistant to EAE and resistance was associated with a strongly diminished production of IFN-γ by myelin-reactive CD4+ T cells 58. Our results suggest that this phenotype may be partly due to a reduced amplification of chemotactic and maturation signals by DAP12-associated receptors, resulting in an inadequate T cell priming in vivo.
Human TREM-2 is the first DAP12-associated receptor identified on DCs. TREM-2 is expressed on immature monocyte-derived DCs, but not on mature DCs or primary blood DCs. In addition, mouse TREM-2 transcripts were recently observed in cultured macrophage cell lines 54. Thus, more DAP12-associated receptors are likely to be expressed on blood and tissues DCs. In addition, such receptors might be expressed not only in immature DCs, but also in mature DCs, regulating critical functions, such as IL-12 secretion. To fully understand the physiological functions of DAP12 in DCs, it will be important to identify all the DAP12-associated DC receptors, their level of expression in different maturation stages, and their ligands.
We thank Rachel Ettinger, Greg Klein, and Fraser McBlane for reviewing the manuscript, and Lena Angman for technical assistance.
The Basel Institute for Immunology was founded and is supported by Hoffmann-LaRoche Ltd., CH-4002 Basel.
M. Cella's present address is Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Ave., St. Louis, MO 63110.
Abbreviations used in this paper: CCR7, CC chemokine receptor 7; DC, dendritic cell; EMSA, electrophoretic mobility assay; ERK, extracellular signal–regulated kinase; HRP, horseradish peroxidase; ITAM, immunoreceptor tyrosine-based activation motif; MAPK, mitogen-activated protein kinase; MDL-1, myeloid DAP12-associating lectin-1; NF, nuclear factor; PTK, protein tyrosine kinase; SAPK, stress-activated protein kinase; SIRP-β, signal-regulatory protein β; TLR, Toll-like receptor; TREM, triggering receptor expressed on myeloid cells.